LINC02290 long intergenic non-protein coding RNA 2290
Information
- Symbol
- LINC02290
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2290
- Entrez Gene ID
- 105370540
- Genome
- hg19
- Position
- chr14:66,578,299-66,595,548
- Genome
- hg38
- Position
- chr14:66,111,581-66,128,830
- HGNC
- HGNC:53206 HGNC
- Ensembl
- ENSG00000258502 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
---|
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000666006.1 | hg38 | chr14 | 66,111,557 | 66,128,052 | 16,496 |
ENST00000667482.1 | hg38 | chr14 | 66,111,581 | 66,128,830 | 17,250 |
ENST00000666006.1 | hg19 | chr14 | 66,578,275 | 66,594,770 | 16,496 |
ENST00000667482.1 | hg19 | chr14 | 66,578,299 | 66,595,548 | 17,250 |
Genome browser